National Society for Phenylketonuria (NSPKU)

Phenylketonuria (PKU) is a rare inherited condition in which there is a build up of phenylalanine in the body. Phenylalanine is a natural substance; it is a building block of protein. PKU is looked for in all newborns in the United Kingdom by measuring phenylalanine levels in the heel-prick blood test. All babies should have this test as it allows treatment to start early in life.

The National Society for Phenylketonuria (NSPKU) offers help and support for people with phenylketonuria, their families and carers.

Who to contact

Telephone
Helpline: 030 3040 1090
Email
info@nspku.org
Website
The National Society for Phenylketonuria 

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